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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593376Generated: October 30, 2026

Tetrahydrofuran → HCID 68691135, compound

https://huagongshe.com/reaction/1593376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 68690920HCID 68690920—
SolventMethanolHCID 887—
ProductHCID 68691135HCID 68691135—

Reaction Steps

Into 20 ml of THF and 6 ml of methanol was dissolved 5.17 g of 4-[(2S,5R)-4-benzyl-2,5-dimethylpiperazin-1-yl]-2-fluorobenzonitrile, and then 9.83 g of potassium t-butoxide was added thereto, followed by stirring at room temperature overnight. A saturated ammonium chloride aqueous solution was added to the reaction solution, followed by extraction with chloroform. After the organic layer was dried over anhydrous sodium sulfate, the solvent was removed by evaporation and the resulting residue was purified by silica gel column chromatography to obtain 4.72 g of the title compound from an eluate eluted with hexane-ethyl acetate (80:20, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297698B2
Source datasetuspto-grants-2007_11
ORD IDord-6912e1b17be049c09feecb0040666133
Source noteuspto-grants-2007_11